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| Name | Class |
|---|---|
| University of Miami | OTHER |
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Despite advances in HIV prevention, the HIV incidence among young men who have sex with men (YMSM) is increasing, threatening to derail achievement of the United States End the HIV Epidemic goals. Although, pre-exposure prophylaxis (PrEP) is a highly effective HIV prevention method, adherence was sufficiently low to comprise efficacy among a high proportion of YMSM in multiple clinical trials and demonstration projects. In this study, the investigators will leverage a novel urine point-of-care drug-level test for PrEP adherence, to both enhance and target motivational-interviewing-based adherence counseling among YMSM, with the goal of preventing HIV infections among this critically at-risk group.
Young men who have sex with men (YMSM; ages 15-29 years) have rising HIV incidence in the United States. Pre-exposure prophylaxis (PrEP) is a highly effective medication prevent HIV infection, both at the individual and population level. However, in several clinical trials and demonstration projects among YMSM, a majority of participants had adherence to PrEP sufficiently low to compromise efficacy throughout the study. Unfortunately, pill-counts and self-reported adherence have limitations in this population, and therapeutic drug monitoring using previously available methods requires expensive equipment and specialized staff, meaning it cannot be implemented at the point-of-care (POC). The investigators have developed a novel POC test to measure urine drug-levels to PrEP for the first time, providing the opportunity to target and enhance adherence counseling during a routine clinical visit. Substantial knowledge gaps on the correct counseling approach and framing of the drug-level feedback message must be addressed to use this strategy to improve adherence among YMSM. This study will use a mixed methods approach to test the central hypothesis that an intervention leveraging a POC urine bioassay to detect PrEP adherence can both target and enhance adherence counseling. Brief interventions are a motivational interviewing (MI) counseling approach with wide uptake by primary care providers for substance use prevention and medical therapy adherence. PrEP2-BAY proposes a brief intervention be used as the framework for POC drug-level feedback among YMSM using PrEP. This study will test the acceptability, feasibility, and preliminary impact on long-term adherence, measured through hair tenofovir levels, of the brief intervention in a pilot randomized controlled trial among YMSM. This proposed research plan has the goal of optimizing PrEP's impact through a novel adherence support intervention. The findings of this proposal will lead to a R01 application to test a POC bioassay-enhanced adherence brief intervention among YMSM in a multi-city trial, with the goal of reducing the burden of HIV among MSM.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention Arm | Experimental | POC adherence testing by a urine tenofovir assay with motivational interviewing counselling |
|
| Standard of Care | No Intervention | Adherence counselling provided by the participant's PrEP care provider |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Motivational Interviewing Counselling | Behavioral | Motivational interviewing-based counseling will be provided to the participant based on the results of the urine test |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants Indicating the Intervention Was Acceptable | Number of participants reporting the intervention to be "somewhat" or "very" acceptable on a five-point Likert scale | 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Long-term Adherence Outcomes | Measure change in tenofovir levels in hair samples from baseline to 3 months using liquid chromatography-mass spectrometry assays. | 3 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Matthew Spinelli, MD, MAS | University of California, San Francisco | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of California, San Francisco/San Francisco General Hospital | San Francisco | California | 94110 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 33527128 | Background | Stalter RM, Baeten JM, Donnell D, Spinelli MA, Glidden DV, Rodrigues WC, Wang G, Vincent M, Mugo N, Mujugira A, Marzinke M, Hendrix C, Gandhi M; Partners PrEP Study Team. Urine Tenofovir Levels Measured Using a Novel Immunoassay Predict Human Immunodeficiency Virus Protection. Clin Infect Dis. 2021 Feb 1;72(3):486-489. doi: 10.1093/cid/ciaa785. | |
| 32167963 |
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We will share de-identified data in publicly accessible databases once study is complete and study findings disseminated.
48 months from start of study
Investigators conducting PrEP research who contact the Principal Investigator
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63 participants were enrolled and randomized.
Participants were recruited via targeted advertisements on a geospatial social mobile application.
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| ID | Title | Description |
|---|---|---|
| FG000 | Intervention Arm | POC adherence testing by a urine tenofovir assay with motivational interviewing counselling |
| FG001 | Standard of Care | Adherence counselling provided by the participant's PrEP care provider |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
One participant from the intervention arm did not complete the study and was lost to follow-up. One participant from the intervention arm and one participant from the standard of care arm were excluded from analysis due to inadequate hair samples.
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| ID | Title | Description |
|---|---|---|
| BG000 | Intervention Arm | POC adherence testing by a urine tenofovir assay with motivational interviewing counselling |
| BG001 | Standard of Care | Adherence counselling provided by the participant's PrEP care provider |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Sex: Female, Male | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Number of Participants Indicating the Intervention Was Acceptable | Number of participants reporting the intervention to be "somewhat" or "very" acceptable on a five-point Likert scale | One participant did not complete the study and was lost to follow-up. One participant was excluded from analysis due to inadequate hair samples. | Posted | Count of Participants | Participants | 3 months |
|
|
From enrollment until end of follow-up, up to 4 months
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Intervention Arm | POC adherence testing by a urine tenofovir assay with motivational interviewing counselling |
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Limitations of this study include the small sample size, short follow-up, and inability to assess downstream HIV incidence. Additionally, generalizability may be limited to YMSM engaged via app-based recruitment and willing to self-collect samples. Larger, longer-term RCTs should be completed next to establish efficacy and implementation strategies.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Matthew Spinelli | University of California, San Francisco | 415-476-4082 | matthew.spinelli@ucsf.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Oct 7, 2022 | Jan 12, 2026 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D040242 | Risk Reduction Behavior |
| ID | Term |
|---|---|
| D001519 | Behavior |
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| Point-of-care Urine Tenofovir Measurement | Device | Urine will be collected and the presence or absence of tenofovir will be measured with the point-of-care urine tenofovir test. |
|
| Spinelli MA, Rodrigues WC, Wang G, Vincent M, Glidden DV, Okochi H, Stalter R, Defechereux P, Deutsch M, Grant RM, Ngure K, Mugo NR, Baeten JM, Gandhi M; Partners PrEP Study Team. Brief Report: High Accuracy of a Real-Time Urine Antibody-Based Tenofovir Point-of-Care Test Compared With Laboratory-Based ELISA in Diverse Populations. J Acquir Immune Defic Syndr. 2020 Jun 1;84(2):149-152. doi: 10.1097/QAI.0000000000002322. |
| 31634188 | Background | Gandhi M, Wang G, King R, Rodrigues WC, Vincent M, Glidden DV, Cressey TR, Bacchetti P, Spinelli MA, Okochi H, Siriprakaisil O, Klinbuayaem V, Mugo NR, Ngure K, Drain PK, Baeten JM. Development and validation of the first point-of-care assay to objectively monitor adherence to HIV treatment and prevention in real-time in routine settings. AIDS. 2020 Feb 1;34(2):255-260. doi: 10.1097/QAD.0000000000002395. |
| 30649051 | Background | Spinelli MA, Glidden DV, Rodrigues WC, Wang G, Vincent M, Okochi H, Kuncze K, Mehrotra M, Defechereux P, Buchbinder SP, Grant RM, Gandhi M. Low tenofovir level in urine by a novel immunoassay is associated with seroconversion in a preexposure prophylaxis demonstration project. AIDS. 2019 Apr 1;33(5):867-872. doi: 10.1097/QAD.0000000000002135. |
| BG002 | Total | Total of all reporting groups |
| Participants |
|
| Age, Continuous | Mean | Standard Deviation | Years |
|
| Daily PrEP Regimen | PrEP medication that participants were clinically prescribed. | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
|
|
| Secondary | Long-term Adherence Outcomes | Measure change in tenofovir levels in hair samples from baseline to 3 months using liquid chromatography-mass spectrometry assays. | One participant from the intervention arm did not complete the study and was lost to follow-up. One participant from the intervention arm and one participant from the standard of care arm were excluded from analysis due to inadequate hair samples. | Posted | Mean | Standard Error | ng/mg | 3 months |
|
|
|
| 0 |
| 42 |
| 0 |
| 42 |
| 0 |
| 42 |
| EG001 | Standard of Care | Adherence counselling provided by the participant's PrEP care provider | 0 | 21 | 0 | 21 | 0 | 21 |
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